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Dutasteride
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Dutasteride reference materials. Our portfolio includes both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine derivatives (N-NO products). These reference standards play a crucial role in pharmaceutical R&D, aiding in formulation development, ANDA/DMF submissions, quality control, method validation, stability studies, and impurity profiling—including the identification and assessment of potentially genotoxic impurities.
Each Dutasteride-related product is rigorously characterized and delivered with a detailed Certificate of Analysis (COA) and comprehensive analytical data to ensure regulatory compliance. Upon request, we also offer EP/USP traceable standards. To maintain the highest quality standards, all materials are subject to periodic re-testing and continuous quality monitoring.
Dutasteride
Dutasteride EP Impurity A
Dutasteride EP Impurity B
Dutasteride EP Impurity C
Dutasteride EP Impurity D
Dutasteride EP Impurity E
Dutasteride EP Impurity F
Dutasteride EP Impurity G
Dutasteride EP Impurity H
Dutasteride EP Impurity I
Dutasteride Dihydro Impurity
Dutasteride Impurity 1
Dutasteride Impurity 2
Desmethyl-6,8,10-triene Dutasteride
Dutasteride Beta-Isomer
Dutasteride Impurity 3
